Chen Jun-An, Voigt Jana, Gilchrist Mike, Papalopulu Nancy, Amaya Enrique
Wellcome Trust/Cancer Research UK Gurdon Institute, Tennis Court Road, Cambridge CB2 1QN, UK.
Mech Dev. 2005 Mar;122(3):307-31. doi: 10.1016/j.mod.2004.11.008.
The formation of mesoderm is an important developmental process of vertebrate embryos, which can be broken down into several steps; mesoderm induction, patterning, morphogenesis and differentiation. Although mesoderm formation in Xenopus has been intensively studied, much remains to be learned about the molecular events responsible for each of these steps. Furthermore, the interplay between mesoderm induction, patterning and morphogenesis remains obscure. Here, we describe an enhanced functional screen in Xenopus designed for large-scale identification of genes controlling mesoderm formation. In order to improve the efficiency of the screen, we used a Xenopus tropicalis unique set of cDNAs, highly enriched in full-length clones. The screening strategy incorporates two mesodermal markers, Xbra and Xmyf-5, to assay for cell fate specification and patterning, respectively. In addition we looked for phenotypes that would suggest effects in morphogenesis, such as gastrulation defects and shortened anterior-posterior axis. Out of 1728 full-length clones we isolated 82 for their ability to alter the phenotype of tadpoles and/or the expression of Xbra and Xmyf-5. Many of the clones gave rise to similar misexpression phenotypes (synphenotypes) and many of the genes within each synphenotype group appeared to be involved in similar pathways. We determined the expression pattern of the 82 genes and found that most of the genes were regionalized and expressed in mesoderm. We expect that many of the genes identified in this screen will be important in mesoderm formation.
中胚层的形成是脊椎动物胚胎重要的发育过程,可细分为几个步骤:中胚层诱导、模式形成、形态发生和分化。尽管非洲爪蟾中胚层的形成已得到深入研究,但对于这些步骤中每一步所涉及的分子事件仍有许多有待了解之处。此外,中胚层诱导、模式形成和形态发生之间的相互作用仍不清楚。在此,我们描述了一种在非洲爪蟾中进行的增强功能筛选,旨在大规模鉴定控制中胚层形成的基因。为了提高筛选效率,我们使用了一组非洲爪蟾特有的cDNA,这些cDNA高度富集全长克隆。筛选策略纳入了两个中胚层标记物Xbra和Xmyf-5,分别用于检测细胞命运特化和模式形成。此外,我们寻找了可能提示对形态发生有影响的表型,如原肠胚形成缺陷和前后轴缩短。在1728个全长克隆中,我们分离出了82个,因其能够改变蝌蚪的表型和/或Xbra和Xmyf-5的表达。许多克隆产生了相似的错误表达表型(共表型),并且每个共表型组中的许多基因似乎参与了相似的信号通路。我们确定了这82个基因的表达模式,发现大多数基因在中胚层中呈区域化表达。我们预计,在此筛选中鉴定出的许多基因在中胚层形成过程中都将具有重要作用。